NDC 15631-0063

AURUM BROMATUM

Aurum Bromatum

AURUM BROMATUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Gold Tribromide.

Product ID15631-0063_700e0ef0-2dc5-4e12-94a3-516259265e8b
NDC15631-0063
Product TypeHuman Otc Drug
Proprietary NameAURUM BROMATUM
Generic NameAurum Bromatum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGOLD TRIBROMIDE
Active Ingredient Strength4 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0063-0

100 PELLET in 1 PACKAGE (15631-0063-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0063-5 [15631006305]

AURUM BROMATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0063-2 [15631006302]

AURUM BROMATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0063-0 [15631006300]

AURUM BROMATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0063-4 [15631006304]

AURUM BROMATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0063-1 [15631006301]

AURUM BROMATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0063-3 [15631006303]

AURUM BROMATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

Drug Details

Active Ingredients

IngredientStrength
GOLD TRIBROMIDE4 [hp_X]/1

OpenFDA Data

SPL SET ID:d4a957a6-a1c1-4aab-b32f-8c63193cfa15
Manufacturer
UNII

NDC Crossover Matching brand name "AURUM BROMATUM" or generic name "Aurum Bromatum"

NDCBrand NameGeneric Name
15631-0063AURUM BROMATUMAURUM BROMATUM
63545-292Aurum BromatumAurum Bromatum
63545-293Aurum BromatumAurum Bromatum
63545-294Aurum BromatumAurum Bromatum
63545-295Aurum BromatumAurum Bromatum
63545-296Aurum BromatumAurum Bromatum
63545-297Aurum BromatumAurum Bromatum
63545-298Aurum BromatumAurum Bromatum
68428-238Aurum bromatumGOLD TRIBROMIDE
71919-099Aurum bromatumGOLD TRIBROMIDE

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